Fill-finish process for peptide solutions

ABSTRACT

The enclosed disclosure describes, among other things, a method including the steps of a first deaerating step in which a mixture comprising peptides is deaerated by lowering the pressure, filtering the mixture through a sterilizing filter; and a second deaerating step, in which the filtrate is deaerated by vibration and lowering the pressure.

BACKGROUND OF THE INVENTION

Purified protein and/or peptide mixtures can be administered to patients for a variety of therapeutic uses. A peptide solution prepared for application to patients must be sterilized prior to use. The purification and packaging of peptides, and biotech products in general, can be exceptionally difficult. The products are complex, may be sensitive to light, temperature, pressure, pH, radiation, mechanical disturbances and otherwise sensitive to environmental conditions. Furthermore, the products may physically change or degrade easily, even under ideal processing conditions. A suitable sterilization process for some proteins (including oligopeptides) includes filtration of a peptide solution. The filter can be sized to retain (i.e., remove from the peptide solution) particulates, microorganisms, and viruses, while the proteins are able to pass through the membrane.

Accordingly, it would be desirable to develop a method of filtering and packaging a peptide solution in a manner that does not substantially damage the peptides, yet which method still permits a suitably high process throughput (i.e., filtration rate) over time. Additionally, it would be desirable to develop a filtering method generally applicable to any protein, such that the general peptide can be filtered (e.g., sterile filtered) at an efficient rate without incurring substantial damage to/loss of the peptide.

SUMMARY OF THE INVENTION

In various embodiments, the present invention includes a method to manufacture and purify peptide solutions. In some embodiments, the methods include steps of: a first deaerating step wherein a mixture comprising peptides is deaerated by lowering the pressure, filtering the mixture through a sterilizing filter, and a second deaerating step, wherein the filtrate is deaerated by vibration and lowering the pressure.

In some embodiments, methods to manufacture and purify peptide solutions of the present invention do not include filtering the mixture through a sterilizing filter. Indeed, in some embodiments, one aspect of the invention is the recognition that certain particular peptide solutions may have characteristics that render them amenable to particular preparation methodologies that may or may not be effective for other peptide solutions. In some embodiments, methods that do not utilize filtering are desirable. Alternatively or additionally, in some embodiments, provided methods to manufacture and purify peptide solutions of the present invention include heat sterilization without filtration. In some embodiments, the present invention encompasses the recognition that certain peptide solutions that do not require filtration are amenable to manufacture and/or purification using methods that include heat sterilization and/or that do not include filtration.

In some embodiments, methods that includes a filtering step utilize a sterilizing filter that has an average pore size is less than about 0.45 μm.

In some embodiments, the first deaerating step comprises lowering the pressure of the mixture at a rate of less than about −0.1 MPa/min. In some embodiments, the first deaerating step comprises lowering the pressure by about at least −0.05 MPa. In some embodiments, the lower pressure is maintained for at least about 30 minutes.

In some embodiments, the second deaerating step comprises vibrating the mixture at 150 revolutions per minute and the eccentric distance of the vibration motion is between position numbers 6 and 8. In some embodiments, the second deaerating step comprises lowering the pressure by about at least −0.05 MPa.

In some embodiments, the method further includes mixing peptides with a solvent before the first deaerating step.

In some embodiments, utilized peptide solutions are RADA-16 (SEQ ID NO: 1) peptide solutions. In some embodiments, utilize peptide solutions are or comprise an IEIK13 (SEQ ID NO: 39) peptide solution. In some embodiments, utilized peptide solutions are solutions of a peptide that appears in Table 1. In some embodiments, utilized peptide solutions are solutions of a peptide that appears in Table 2. In some embodiments, utilized peptide solutions are solutions of two or more peptides.

In some particular embodiments, the present invention provides methods to manufacture and purify IEIK13 (SEQ ID NO:39) that lack one or more filtering steps. In some embodiments, the present invention provides methods to manufacture and purify IEIK13 (SEQ ID NO:39) that do not include any filtering steps. One feature of the invention is its recognition that, at least for certain IEIK13 (SEQ ID NO:39) solutions, such filtering may not be required for sterilization.

In some embodiments, the solvent is water. In some embodiments, the method further includes aseptically filling articles with the mixture after the second deaerating step. In some embodiments, the articles are filled at least 5 hours after the second deaerating step. In some embodiments, the articles are filled at a rate of at least about 2 articles/minute, about 3 articles/minute, about 4 articles/minute, about 5 articles/minute, about 6 articles/minute, about 7 articles/minute, about 8 articles/minute, about 9 articles/minute, about 10 articles/minute, about 11 articles/minute, about 12 articles/minute, about 13 articles/minute, about 14 articles/minute, about 15 articles/minute, about 16 articles/minute, about 17 articles/minute, about 18 articles/minute, about 19 articles/minute, or about 20 articles/minute, or a multiple thereof; in some embodiments, the articles are filled at a rate of about 100, 200, 300, 400, 500, 600, 700, 800, 900, or about 1000 or more articles/hour.

In some embodiments, a high speed filling machine (e.g., such as FLS 3000, Bosch; 1I/1F/1I1VI0CY, 8I/8F/8IS-CY or 10I/10FF/10I, (KT Manufacturing Co. Ltd.) is utilized to fill the articles; in some embodiments, the high speed filling machine is or comprises a plurality of filling nozzles (e.g., 2, 3, 4, 5, etc.). In some embodiments, the machine is arranged and constructed so that each nozzle has a capacity to fill articles at a rate of at least about 2 articles/minute, about 3 articles/minute, about 4 articles/minute, about 5 articles/minute, about 6 articles/minute, about 7 articles/minute, about 8 articles/minute, about 9 articles/minute, about 10 articles/minute, about 11 articles/minute, about 12 articles/minute, about 13 articles/minute, about 14 articles/minute, about 15 articles/minute, about 16 articles/minute, about 17 articles/minute, about 18 articles/minute, about 19 articles/minute, or about 20 articles/minute or at a rate of about 100, 200, 300, 400, 500, 600, 700, 800, 900, or about 1000 or more articles/hour, and/or the machine is arranged and constructed (e.g., in some embodiments by virtue of presence of multiple nozzles) to fill articles at a rate of at least about 1000, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000, 10000, 11000, 12000, 13000, 14000 or at least about 15000 articles/hour. In some embodiments, provided methods utilize such a high speed filing machine at least 1%, 2%, 3%, 4%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or at least 100% of its capacity.

In some embodiments, the articles are syringes, pouches, vials, tubes. In some embodiments, the method further includes packaging filled articles with gas permeable materials and a sterilization step after the filling step.

In some embodiments, gas sterilization is performed by ethylene oxide gas. In some embodiments, gas sterilization is performed by hydrogen peroxide gas.

In some embodiments, the article is performed with single packaging.

In some embodiments, the article is performed with double packaging.

In some embodiments, the filtration is performed at a pressure of about 0.1-0.6 mega pascals (MPa). In some certain embodiments, the filtration is performed at a pressure of about 0.1 MPa, about 0.2 MPa, about 0.3 MPa, about 0.4 MPa, about 0.5 MPa, or about 0.6 MPa.

In some embodiments, the filtration is performed at about ambient temperature.

In some embodiments, the filter is constructed from a material selected from the group consisting of the following: cellulose nitrate, cellulose acetate, vinyl polymers, fluorocarbons, polyethylene, ultrahigh molecular weight polyethylene, polypropylene, EVA copolymers and alpha olefins, metallocene olefinic polymers, PFA, MFA, PTFE, polycarbonates, vinyl copolymers, polyamides, nylon, polyesters, cellulose, cellulose acetate, regenerated cellulose, cellulose composites, polysulfone, polyethersulfone, polyarylsulfone, polyphenylsulfone, polyacrylonitrile, polyvinylidene fluoride (PVDF), and blends thereof.

In some embodiments, the filter is constructed from polyethersulfone.

In some embodiments, the filtering step comprises a step of filling the filter at a first pressure, then increasing the pressure to perform the filtration. In some embodiments, additional tank is placed between pressure source and filtration feed tank to keep the pressure as the pressure source to perform the filtration. In some certain embodiments, a first pressure for filing the filter is relatively weak. In some embodiments, a first pressure is below about 0.01 MPa. In some embodiments, a first pressure is about 0.05 MPa.

In some embodiments, the filter is tested for integrity. In some embodiments, the filter is tested for integrity using an using an integrity test instrument (e.g., such as INTEGRITEST®4 System, Millipore; PALLTRONIC® AquaWIT Series Filter Integrity Test System or PALLTRONIC® Flowstar Series Integrity Test Instrument; Pall Corp.; Meissner's ACCUFLUX® Automated Filter Integrity Test Instrument, Meissner Filtration Products).

In some embodiments, the filter is washed prior to an integrity test. In some certain embodiments, the filter is washed with water prior to an integrity test. In some certain embodiments, the filter is washed with hot water and/or by high-pressure water prior to an integrity test. In some certain embodiments, the filter is washed with steam and/or by autoclaving prior to an integrity test.

In some embodiments, the scraper is used to feed almost all the solution from filtration feed tank to filter. In some embodiments, the filtration step includes the use of pigs to aide filtration. In some embodiments, the filtration step is performed in two filters operated in parallel. In some embodiments, the method further includes a cleaning step, which comprises adding steam to the filtration and deaeration equipment.

Definitions

By “complementary” is meant capable of forming ionic or hydrogen bonding interactions between hydrophilic residues from adjacent peptides in the scaffold, each hydrophilic residue in a peptide either hydrogen bonds or ionically pairs with a hydrophilic residue on an adjacent peptide or is exposed to solvent.

By “structurally compatible” is meant capable of maintaining a sufficiently constant intrapeptide distance to allow scaffold formation. In certain embodiments of the invention the variation in the intrapeptide distance is less than 4, 3, 2, or 1 angstroms. It is also contemplated that larger variations in the intrapeptide distance may not prevent scaffold formation if sufficient stabilizing forces are present. This distance may be calculated based on molecular modeling or based on a simplified procedure that has been previously reported (U.S. Pat. No. 5,670,483). In this method, the intrapeptide distance is calculated by taking the sum of the number of unbranched atoms on the side-chains of each amino acid in a pair. For example, the intrapeptide distance for a lysine-glutamic acid ionic pair is 5+4=9 atoms, and the distance for a glutamine-glutamine hydrogen bonding pair is 4+4=8 atoms. Using a conversion factor of 3 angstroms per atom, the variation in the intrapeptide distance of peptides having lysine-glutamic acid pairs and glutamine-glutamine pairs (e.g., 9 versus 8 atoms) is 3 angstroms.

The term “pure” is used to indicate the extent to which the peptides described herein are free of other chemical species, including deletion adducts of the peptide in question and peptides of differing lengths.

As used herein, a hydrogel such as a peptide hydrogel is “stable with respect to mechanical or physical agitation” if, when subjected to mechanical agitation, it substantially retains the physical properties (such as elasticity, viscosity, etc.), that characterized the hydrogel prior to physical agitation. The hydrogel need not maintain its shape or size and may fragment into smaller pieces when subjected to mechanical agitation while still being termed stable with respect to mechanical or physical agitation. The term “stable” does not have this meaning except when used with this phrase.

As used herein, the term “nanofiber” refers to a fiber having a diameter of nanoscale dimensions. Typically a nanoscale fiber has a diameter of 500 nm or less. According to certain embodiments of the invention a nanofiber has a diameter of less than 100 nm. According to certain other embodiments of the invention a nanofiber has a diameter of less than 50 nm. According to certain other embodiments of the invention a nanofiber has a diameter of less than 20 nm. According to certain other embodiments of the invention a nanofiber has a diameter of between 10 and 20 nm. According to certain other embodiments of the invention a nanofiber has a diameter of between 5 and 10 nm. According to certain other embodiments of the invention a nanofiber has a diameter of less than 5 nm.

DETAILED DESCRIPTION OF CERTAIN EMBODIMENTS OF THE INVENTION

The purification and packaging of peptides, and biotech products in general, can be exceptionally difficult. The products are complex, may be sensitive to light, temperature, pressure, pH, radiation, mechanical disturbances and otherwise sensitive to environmental conditions. Furthermore, the products may physically change or degrade easily, even under ideal processing conditions.

We have discovered a series of processes to enable sterilization and packaging of peptide mixtures, including self-assembling peptides mixtures. The provided methods do not utilize thermal, chemical and radiation methods for sterilization as they can degrade peptides. According to the present invention, filtration is a particularly useful method of sterilization of the peptide mixtures.

In one aspect, the invention encompasses the recognition that relying on a physical sterilization method poses problems based on the rheology of the peptide mixtures. For example, the viscosity of the peptides mixtures can change over time, or simply be very high, such looking like a gel. Provided techniques are particular useful in the purification of self-assembling peptides, which can pose particular difficulties. The present invention encompasses the discovery of a series of operations and operating conditions that can (a) produce a sterilized peptide mixture, (b) fill and sterilize packages (e.g., syringes) a the peptide mixture and/or (c) clean the processing equipment to current good manufacturing practices (cGMP). In some embodiments, the inventive filtration equipment utilizes a micron size filter (e.g., 0.2 micron polyethersulfone filter, though other sizes and materials of construction are applicable). In some embodiments, the provided filtration methods include “pre-coating” the filter (i.e., filling the filter with the media to completely cover the filter surface by removing air in filter housing at a lower pressure before increasing the pressure for active filtration). In some embodiments, provided filtration methods involve the use of a pipeline aide (e.g., a “pig”) or some other mechanical means (e.g., scraping) to ensure that the maximum quantity of the peptide mixture passes through the filter. In some embodiments, provided filtration method are preceded by a deaerating step (e.g., deaeration by pressure reduction). In some embodiments, provided filtration methods are followed by a deaerating step (e.g., deaeration by vibration). In some embodiments, provided filtration method includes integrity test procedure of sterilizing filter after filtering. In some embodiments, sterilization of surface of syringes filled with peptide mixture include the use of germicidal gas (e.g., ethylene oxide, hydrogen peroxide) to avoid degradation of peptide solution in the syringe.

Self-Assembling Peptides

Peptide sequences appropriate for use with the invention include those reported in U.S. Pat. Nos. 5,670,483 and 5,955,343, and U.S. patent application Ser. No. 09/778,200, the contents of all of which are incorporated herein by reference. These peptide chains consist of alternating hydrophilic and hydrophobic amino acids that are capable of self-assembling to form an exceedingly stable beta-sheet macroscopic structure in the presence of electrolytes, such as monovalent cations. The peptide chains are complementary and structurally compatible. The side-chains of the peptide chains in the structure partition into two faces, a polar face with charged ionic side chains and a nonpolar face with alanines or other hydrophobic groups. These ionic side chains are self-complementary to one another in that the positively charged and negatively charged amino acid residues can form complementary ionic pairs. These peptide chains are therefore called ionic, self-complementary peptides, or Type I self-assembling peptides. If the ionic residues alternate with one positively and one negatively charged residue (−+−+−+−+), the peptide chains ae described as “modulus I;” if the ionic residues alternate with two positively and two negatively charged residues (−−++−−++), the peptide chains are described as “modulus II.” Exemplary peptide sequences for use with the invention include those listed in Table 1. In some embodiments, peptide sequences for use with the invention have at least 12 or 16 amino acid residues. Both D- and L-amino acids may be used to produce peptide chains. They may be mixed in the same chain, or peptide compositions may be prepared having mixtures of individual chains that themselves only include D- and L-amino acids.

TABLE 1 Representative Self Assembling Peptides Name Sequence (n-->c) Modulus RADA16-I n-RADARADARADARADA-c I SEQ ID NO: 1 RGDA16-I n-RADARGDARADARGDA-c I SEQ ID NO: 2 RADA8-I n-RADARADA-c I SEQ ID NO: 3 RAD16-II n-RARADADARARADADA-c II SEQ ID NO: 4 RAD8-II n-RARADADA-c II SEQ ID NO: 5 EAKA16-I n-AEAKAEAKAEAKAEAK-c I SEQ ID NO: 6 EAKA8-I n-AEAKAEAK-c I SEQ ID NO: 7 RAEA16-I n-RAEARAEARAEARAEA-c I SEQ ID NO: 8 RAEA8-I n-RAEARAEA-c I SEQ ID NO: 9 KADA16-I n-KADAKADAKADAKADA-c I SEQ ID NO: 10 KADA8-I n-KADAKADA-c I SEQ ID NO: 11 KLD12 n-KLDLKLDLKLDL-c SEQ ID NO: 12 EAH16-II n-AEAEAHAHAEAEAHAH-c II SEQ ID NO: 13 EAH8-II n-AEAEAHAH-c II SEQ ID NO: 14 EFK16-II n-FEFEFKFKFEFEFKFK-c II SEQ ID NO: 15 EFK8-II n-FEFKFEFK-c I SEQ ID NO: 16 KFE12 n-FKFEFKFEFKFE-c SEQ ID NO: 17 KFE8 n-FKFEFKFE-c SEQ ID NO: 18 KFE16 n-FKFEFKFEFKFEFKFE-c SEQ ID NO: 19 KFQ12 n-FKFQFKFQFKFQ-c SEQ ID NO: 20 KIE12 n-IKIEIKIEIKIE-c SEQ ID NO: 21 KVE12 n-VKVEVKVEVKVE-c SEQ ID NO: 22 ELK16-II n-LELELKLKLELELKLK-c II SEQ ID NO: 23 ELK8-II n-LELELKLK-c II SEQ ID NO: 24 EAK16-II n-AEAEAKAKAEAEAKAK-c II SEQ ID NO: 25 EAK12 n-AEAEAEAEAKAK-c IV/ SEQ ID NO: 26 II EAK8-II n-AEAEAKAK-c II SEQ ID NO: 27 KAE16-IV n-KAKAKAKAEAEAEAEA-c IV SEQ ID NO: 28 EAK16-IV n-AEAEAEAEAKAKAKAK-c IV SEQ ID NO: 29 RAD16-IV n-RARARARADADADADA-c IV SEQ ID NO: 30 DAR16-IV n-ADADADADARARARAR-c IV SEQ ID NO: 31 DAR16-IV* n-DADADADARARARARA-c IV SEQ ID NO: 32 DAR32-IV n-(ADADADADARARA IV SEQ ID NO: 33 RAR)₂-c EHK16 n-HEHEHKHKHEHEH N/A SEQ ID NO: 34 ICHK-c EHK8-I n-HEHEHKHK-c N/A SEQ ID NO: 35 VE20* n-VEVEVEVEVEVEVEVE N/A SEQ ID NO: 36 VEVE-c RF20* n-RFRFRFRFRFRFRFRF N/A SEQ ID NO: 37 RFRF-c IEIK9 n-IEIKIEIKI-c I SEQ ID NO: 38 IEIK13 n-IEIKIEIKIEIKI-c I SEQ ID NO: 39 N/A denotes not applicable *These peptides form a β-sheet when incubated in a solution containing NaCl, however they have not been observed to self-assemble to form macroscopic scaffolds.

Many modulus I and II self-complementary peptide sequences, such as EAK16, KAE16, RAD16, RAE16, and KAD16, have been analyzed previously (Table 1). Modulus IV ionic self-complementary peptide sequences containing 16 amino acids, such as EAK16-IV, KAE16-IV, DAR16-IV and RAD16-IV, have also been studied. If the charged residues in these self-assembling peptide chains are substituted (i.e., the positive charged lysines are replaced by positively charged arginines and the negatively charged glutamates are replaced by negatively charged aspartates), there are essentially no significant effects on the self-assembly process. However, if the positively charged resides, lysine and arginine are replaced by negatively charged residues, aspartate and glutamate, the peptide chains can no longer undergo self-assembly to form macroscopic scaffolds; however, they can still form a beta-sheet structure in the presence of salt. Other hydrophilic residues, such as asparagine and glutamine, that form hydrogen-bonds may be incorporated into the peptide chains instead of, or in addition to, charged residues. If the alanines in the peptide chains are changed to more hydrophobic residues, such as leucine, isoleucine, phenylalanine or tyrosine, these peptide chains have a greater tendency to self-assemble and form peptide matrices with enhanced strength. Some peptides that have similar compositions and lengths as the aforementioned peptide chains form alpha-helices and random-coils rather than beta-sheets and do not form macroscopic structures. Thus, in addition to self-complementarity, other factors are likely to be important for the formation of macroscopic scaffolds, such as the chain length, the degree of intermolecular interaction, and the ability to form staggered arrays.

Other self-assembling peptide chains may be generated by changing the amino acid sequence of any self-assembling peptide chains by a single amino acid residue or by multiple amino acid residues. Additionally, the incorporation of specific cell recognition ligands, such as RGD or RAD, into the peptide scaffold may promote the proliferation of the encapsulated cells. In vivo, these ligands may also attract cells from outside a scaffold to the scaffold, where they may invade the scaffold or otherwise interact with the encapsulated cells. To increase the mechanical strength of the resulting scaffolds, cysteines may be incorporated into the peptide chains to allow the formation of disulfide bonds, or residues with aromatic rings may be incorporated and cross-linked by exposure to UV light. The in vivo half-life of the scaffolds may also be modulated by the incorporation of protease cleavage sites into the scaffold, allowing the scaffold to be enzymatically degraded. Combinations of any of the above alterations may also be made to the same peptide scaffold.

Self-assembled nanoscale structures can be formed with varying degrees of stiffness or elasticity. While not wishing to be bound by any theory, low elasticity may be an important factor in allowing cells to migrate into the scaffold and to communicate with one another once resident in the scaffold. The peptide scaffolds described herein typically have a low elastic modulus, in the range of 1-10 kPa as measured in a standard cone-plate rheometer. Such low values permit scaffold deformation as a result of cell contraction, and this deformation may provide the means for cell-cell communication. In addition, such moduli allow the scaffold to transmit physiological stresses to cells migrating therein, stimulating the cells to produce tissue that is closer in microstructure to native tissue than scar. Scaffold stiffness can be controlled by a variety of means including changes in peptide sequence, changes in peptide concentration, and changes in peptide length. Other methods for increasing stiffness can also be used, such as by attaching a biotin molecule to the amino- or carboxy-terminus of the peptide chains or between the amino- and carboxy-termini, which may then be cross-linked.

Peptide chains linked may be synthesized using standard f-moc chemistry and purified using high pressure liquid chromatography. After initial synthesis peptide chains may be preserved for storage by lyophilization. The formation of a peptide scaffold may be initiated by the addition of electrolytes as described herein. The hydrophobic residues with aromatic side chains may be cross-linked by exposure to UV irradiation. The extent of the cross-linking may be precisely controlled by the predetermined length of exposure to UV light and the predetermined peptide chain concentration. The extent of cross-linking may be determined by light scattering, gel filtration, or scanning electron microscopy using standard methods. Furthermore, the extent of cross-linking may also be examined by HPLC or mass spectrometry analysis of the scaffold after digestion with a protease, such as matrix metalloproteases. The material strength of the scaffold may be determined before and after cross-linking, as described herein.

!TABLE 2?!Representative Peptide Sequences?!for Cross-Linking?!Name? Sequence (N-->C) RGDY16 RGDYRYDYRYDYRGDY SEQ ID NO: 40 RGDF16 RGDFRFDFRFDFRGDF SEQ ID NO: 41 RGDW16 RGDWRWDWRWDWRGDW SEQ ID NO: 42 RADY16 RADYRYEYRYEYRADY SEQ ID NO: 43 RADF16 RADFRFDFRFDFRADF SEQ ID NO: 44 RADW16 RADWRWDWRWDWRADW SEQ ID NO: 45

If desired, peptide scaffolds may also formed with a predetermined shape or volume. To form a scaffold with a desired geometry or dimension, an aqueous peptide solution is added to a pre-shaped casting mold, and the peptide chains are induced to self-assemble into a scaffold by the addition of an electrolyte, as described herein. The resulting geometry and dimensions of the macroscopic peptide scaffold are governed by the concentration and amount of peptide solution that is applied, the concentration of electrolyte used to induce assembly of the scaffold, and the dimensions of the casting apparatus.

If desired, peptide scaffolds may be characterized using various biophysical and optical instrumentation, such as circular dichroism (CD), dynamic light scattering, Fourier transform infrared (FTIR), atomic force microscopy (ATM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). For example, biophysical methods may be used to determine the degree of beta-sheet secondary structure in the peptide scaffold. Additionally, filament and pore size, fiber diameter, length, elasticity, and volume fraction may be determined using quantitative image analysis of scanning and transmission electron microscopy. The scaffolds may also be examined using several standard mechanical testing techniques to measure the extent of swelling, the effect of pH and electrolyte concentration on scaffold formation, the level of hydration under various conditions, and the tensile strength.

Aqueous solution of self-assemble peptide is viscous to gel-like, the viscosity of which varies in time. The viscosity of the peptide solution becomes higher and higher when no forces (e.g., shear) is given to the solution. It needs continuous force to keep low viscosity of self-assembling peptide solution. The nature of self-assemble peptide makes formulation more difficult than most liquid formulation. Manufacturing process should be designed for the self-assembling peptide to meet regulatory requirement for medical use and reduce the loss of product in commercial scale manufacturing, as described below.

Dissolution

Synthesized peptides are prepared (e.g., synthesized) by manufacturers and are stored after synthesis in a dried form (e.g., lyophilized). For final purification/sterilization and/or packaging dried peptides should be dissolved in a solvent (e.g., water) at a concentration suitable for the ultimate use/administration.

A dissolution step begins the fill-finish process. In the broadest embodiment, dissolution begins by mixing powdered peptides (e.g., freeze-dried or lyophilized peptides) with water. In some embodiments, the water is bacteriostatic water for injection. In some embodiments, the water is sterile, deionized and/or distilled water. The peptides are dissolved so that the concentration of peptides is between about 0.1 weight percent and about 5 weight percent (e.g., about 0.2 weight percent, about 0.3 weight percent, about 0.4 weight percent, about 0.5 weight percent, about 0.75 weight percent, about 1.0 weight percent, about 1.25 weight percent, about 1.5 weight percent, about 1.75 weight percent, about 2.0 weight percent, about 2.25 weight percent, about 2.5 weight percent, about 2.75 weight percent, and ranges there between). In some embodiments, this concentration is the concentration of the peptides in solution for the final application and/or end use. Final applications or end uses of the peptide solution may influence or determine the concentration at which the peptides are dissolved in solution. In some embodiments, the peptide solution has a concentration of peptides between about 1 weight percent and about 3 weight percent. In calculations of weight percent the moisture content of the peptide powder may be accounted for. In some embodiments, the moisture content of the peptide power is between about 1 weight percent and about 10 weight percent of the peptide powder (e.g., about 5 weight percent).

In some embodiments, peptide power is added to a premeasured amount of water. In some embodiments, peptide power is added slowly or in steps so that one addition of peptides is fully dissolved before a subsequent amount of peptide power is added. Because one objective of the fill-finish process described herein is sterilization of the peptide solution, proper care should be taken to prevent bacterial contamination. Equipment used for dissolution should be autoclaved or steamed, if possible, or sanitized by irradiation (e.g., UV radiation) if autoclaving is not suitable for a particular piece of equipment.

During dissolution, the solution is stirred. Again because of viscosity and dissolution rates, the stirring rate and time are controlled. In some embodiments, the mixer used includes an axial or radial flow impeller and/or a propeller, paddle or turbine shaped impeller. In some embodiments, the mixer is operated at a rate of not less than about 500 rpm, but is brought up to that speed slowly from a stopped speed. For example, the mixer starts at a speed of about 200 rpm as the peptide power is added. Once all of the powder is dissolved the mixer speed is increased to about 500 rpm. The rotational speed of the mixer (either for initial powder addition of for mixing of the dissolved powder) can range from about 30 rpm to about 1000 rpm (e.g., about 50 rpm, about 60 rpm, about 75 rpm, about 100 rpm, about 120 rpm, about 180 rpm, about 240 rpm, about 360 rpm, about 480 rpm about 600 rpm, about 720 rpm, about 840 rpm, about 960 rpm and ranges there between) Those of skill will appreciate that the speed of the mixer depends in large part on the volume of the mixing vessel and according to the speed of the impeller, which in turn depends on the diameter of the impeller. Where v=speed of the impeller and d=the diameter of the impeller, r=rotational speed, the speed can be calculated by v=π*d*r, and should be keep proportional as the vessel size is scaled up.

Once at this speed, mixing continues for about 30 minutes (e.g., about 30 minutes, about 40 minutes, about 45 minutes, about 60 minutes and values there between). The rate of mixer speed is maintained so that the solution is not sheered to such a degree that droplets of the solution are produced from the bulk solution and thrown against the wall of the mixing vessel. The surface of the solution should be continuous, though it does not need to be level, or planar (e.g., a vortex may develop during mixing, however, its surface should be a continuous surface).

During the stirring and dissolution samples are taken from the mixing tank and inspected to monitor the dissolution. The samples are centrifuged to remove any entrained gases. The samples are then visually inspected to ensure dissolution of the peptides, also can be examined with content of dissolved peptide by photometer. If inspection indicates undissolved powder, stirring time can be extended. If inspection indicates dissolution of the peptide powder, the solution may be passed to the next stage of the fill-finish process.

If the solution is substantially completely dissolved the next step in the fill-finish process is to deaerate (e.g., degas) the solution. Our work has shown that a solution that is substantially degassed or deaerated proceeds through filtration in a more efficient manner, with less waste and/or less frequent clogging in the filter.

First Deaeration

As used herein, deaeration is equivalent to degassing, which is a process in which a dissolved or entrained gas (e.g., air) is removed from a liquid, or its quantity in the liquid reduced. The first deaerating step is performed by any acceptable deaerating method. For example, by vacuum, centrifugation, vibration, liquid-gas membrane separation or allowing the solution to degas naturally. In some embodiments, the deaerating step is performed by vacuum (e.g., by altering the pressure on the solution) In some embodiments, applied vacuum is at least −0.01 MPa, −0.015 MPa, −0.02 MPa, −0.025 MPa, −0.03, MPa, −0.035 MPa, −0.04 MPa, −0.045 MPa, −0.05 MPa, −0.055 MPa, −0.06 MPa, −0.065 MPa, −0.07 MPa, −0.075 MPa, −0.08 MPa, −0.085 MPa, −0.09 MPa, −0.095 MPa, −0.098 MPa, −0.099 MPa, −0.1 MPa or more. In some embodiments, applied vacuum is about −0.1 MPa. Among other things, the present invention encompasses the recognition that the rate of reduction of pressure (or increase in vacuum) effects the efficacy and efficiency of the deaerating process as well as the eventual filtration process. In some embodiments, the rate of pressure reduction is not more than about −0.01 MPa/minute (e.g., about −0.005 MPa/minute, about −0.0025 MPa/minute, about −0.001 MPa/minute, and ranges there between). In some embodiments, the rate of pressure reduction is dependent upon the total volume of the solution to be deaerated.

In some embodiments, the deaeration apparatus is equipped with a deaeration chamber for temporarily holding the peptide solution and a suction apparatus for reducing the pressure in the deaeration chamber. The suction apparatus can be of any design or operation to generate a vacuum. In some embodiments, the apparatus may use the dynamic pressure of a water jet, or can be any type of vacuum pump, or the like may be used as the suction apparatus.

It is preferable that a large surface area of the peptide solution inside the deaeration chamber is in contact with the air. Thus, the shape and dimensions of the deaeration chamber can be such to maximize the peptide solution's contact surface area with the air. Further, the flow into the deaeration chamber can be such that the peptide solution circulates along the inner wall of the chamber, maximizing the contact surface area. In some embodiments, the flow of peptide solution into the chamber can be as a thin film along the inner wall of the deaeration chamber. Again, the high surface area (and surface area to volume ratio of the peptide solution) can aide in deaeration efficiency. In some embodiments, however it may be sufficient that the peptide solution is simply allowed to flow into the deaeration chamber. In some particular embodiments, high viscosity (e.g., with viscosity greater than about 15.0 pascal-second [Pa·s]) solutions are allowed to flow into the deaeration chamber.

In some embodiments, solutions are stirred during aeration. In some embodiments, solutions are stirred at a rate of approximately 50 rpm, 100 rpm, 150 rpm, 200 rpm, 250 rpm, 300 rpm, 350 rpm, 400 rpm or 500 rpm. In some embodiments, it is preferable that the peptide solution that has been heated when it is introduced into the deaeration chamber. Such heating may reduce the viscosity of the solution, improving deaeration efficiency. Caution should be taken in heating as some peptides are subject to degradation with heat and therefore heating may not be appropriate in all circumstances.

Stirring can be combined with pressure reduction to efficiently deaerate from viscous peptide mixture but fast stirring might bring babble into the mixture. To dearate from peptide mixture, the mixer is operated at a rate of not less than about 300 rpm. Self-assembling peptide mixture becomes gel-like solution during deaeration if stirring is not done at the same time. Mixing self-assembling peptide solution keeps low viscosity so that the solution is effectively deaerated.

The deaerating step lasts (i.e., the time that vacuum is maintained) for at least about 30 minutes (e.g., about 15 minutes, about 20 minutes, about 40 minutes, about 45 minutes, about 60 minutes). The ultimate length of time for deaerating is dependent on the results, e.g., that the mixture is substantially free of dissolved gas or gas bubbles. During the deaerating samples of the solution are taken and inspected for dissolved gas or bubbles. If dissolved gas or gas bubbles are still present, the degassing process is continued. If the solution is sufficiently free of dissolved gas or bubbles then the fill-finish process can continue.

Filtration

Filters suitable for use according to the disclosed method are not particularly limited and can include surface filters, for example dead-end filters (i.e., in which the fluid to be filtered perpendicularly approaches the filter surface) and cross-flow filters (i.e., in which the fluid to be filtered travels parallel to the filter surface). See, e.g., Kirk-Othmer Encyclopedia of Chemical Technology, vol. 10, pp. 788-853 (“Filtration”) (4th ed., 1993). The filters also are not particularly limited with respect to their classification size (i.e., the size above which dispersed material is retained on the filter and the size below which dispersed material passes into the filtrate). Once a filter classification size is selected for a particular application (i.e., dispersed material to be retained vs. dispersed material to pass into the filtrate), the filter should be operated considering the amount of shear generated by the carrier liquid flowing through the filter relative to the shear sensitivity of the particular protein being filtered.

After the mixture is sufficiently deaerated, the filtration step proceeds. As described above, we have discovered a series of processes to enable sterilization that does not utilize thermal, chemical and radiation methods for sterilization as they can degrade peptides. According to the present invention, filtration is a particularly useful method of sterilization of the peptide mixtures. Filtration is effective in removing residual debris and other small particles as well as sterilizing the peptide solution in a manner that does not result in degradation of the peptides. Filters retain contaminants using two major types of interactions between filters and contaminant particles. Particles are retained due to their size, and may also be retained due to adsorption to the filter material. Molecular and/or electrical forces between the particles and the filter material attract and retain these entities within the filter.

Generally, the pores of the filter are sized to remove at least a portion of contaminants contained in the peptide solution, retaining the removed dispersed contaminants on the upstream side of the filter (e.g., the inlet side) yielding a filtrate substantially free of contaminants. Specifically the filtrate should not contain contaminants in an amount that would adversely affect the use of the purified peptide solution. For examples when the dispersed contaminants include micro-organisms, the filter should be able to remove at least 99.9999% of micro-organisms that originally exists in the solution, that is the sterility assurance level (SAL: 10-) for medical use.

The filter is generally available in various sizes (i.e., filter surface area, for example ranging from about 0.001 m² to about 10 m²) and configurations (e.g., filter discs, filter cartridges). The materials of construction of the filter are selected to be compatible with the peptide mixture (e.g., prevent adherences or excessive friction with the solution). The porous membrane can be formed from materials such as cellulose nitrate, cellulose acetate, vinyl polymers, fluorocarbons, olefins such as polyethylene including ultrahigh molecular weight polyethylene, polypropylene, EVA copolymers and alpha olefins, metallocene olefinic polymers, PFA, MFA, PTFE, polycarbonates, vinyl copolymers such as PVC, polyamides such as nylon, polyesters, cellulose, cellulose acetate, regenerated cellulose, cellulose composites, polysulfone, polyethersulfone, polyarylsulfone, polyphenylsulfone, polyacrylonitrile, polyvinylidene fluoride (PVDF), and blends thereof. Depending on the mixture, the filter may be hydrophilic or hydrophobic. Preferred filters are hydrophilic and are low in protein/peptide binding.

The filtration step is, in some embodiments, performed by filtering through a filter with a specific pore size (e.g., about 0.2 micrometers). The porous membrane includes pores generally having a highly uniform size that is selected depending on the size of the dispersed contaminant to be removed from the liquid mixture. For example, in sterile filtration operations intended to remove microorganisms (while allowing the protein to pass through the filter membrane into the filtrate), the pores preferably have a size in a range of about 0.1 micrometers to about 0.5 micrometers. In some embodiments, the pore size is about 0.15 micrometers, about 0.1 micrometers. Suitable filtration systems can also include a primary filter with a pore size of, e.g., 0.2 micrometers, as well as a coarser prefilter to improve throughput and limit accumulation within the finer filter. The coarser prefilter can have a pore size in the range of about 0.4 micrometers to about 10 micrometers. (e.g., about 0.4 micrometers, about 0.45 micrometers, about 0.5 micrometers, about 0.6 micrometers, about 0.7 micrometers, about 0.8 micrometers, about 1.0 micrometers, about 1.5 micrometers, about 100.0 micrometers). Pre-filter system needs two or more filters so that peptide mixture may be much lost in the pre-filter(s). In addition, tandem pre-filtering system causes to lower the pressure in sterilizing filter, where the initial high pressure is lowered by pre-filter. Highly viscous peptide mixture, such as self-assembling peptide, requires high pressure (0.5 or more mega pascals (MPa)) for filtration, so tandem connection of pre-filter and sterilizing filter is not suitable to manufacturing process of viscous self-assembling peptides.

In various embodiments, filtration according to the present invention is performed at a pressure within a range of about 0.3-0.7, inclusive, for example, about 0.30 MPa, 0.31 MPa, 0.32 MPa, 0.33 MPa, 0.34 MPa, 0.35 MPa, 0.36 MPa, 0.37 MPa, 0.38 MPa, 0.39 MPa, 0.40 MPa, 0.41 MPa, 0.42 MPa, 0.43 MPa, 0.44 MPa, 0.45 MPa, 0.46 MPa, 0.47 MPa, 0.48 MPa, 0.49 MPa, 0.50 MPa, 0.51 MPa, 0.52 MPa, 0.53 MPa, 0.54 MPa, 0.55 MPa; 0.56 MPa, 0.57 MPa, 0.58 MPa, 0.59 MPa, 0.60 MPa, 0.61 MPa, 0.62 MPa, 0.63 MPa, 0.64 MPa, 0.65 MPa, 0.66 MPa, 0.67 MPa, 0.68 MPa, 0.69 MPa, 0.70 MPa. In some embodiments, filtration is performed within a range of about 0.4-0.6 MPa, inclusive. In some embodiments, filtration is performed within a range of about 0.5-0.6 MPa, inclusive. In some embodiments, filtration is performed within a range of about 0.5-0.55 MPa, inclusive.

In some embodiments, filtration according to the present invention is performed at a pressure of about 0.40 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.41 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.42 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.43 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.44 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.45 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.46 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.47 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.48 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.49 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.50 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.51 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.52 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.53 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.54 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.55 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.56 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.57 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.58 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.59 MPa; in some embodiments, filtration according to the present invention is performed at a pressure of about 0.60 MPa.

In some embodiments, pressure is monitored during filtration; in some such embodiments, adjustments may be made to maintain pressure within a desired range. In some embodiments, pressure is monitored sporadically. In some embodiments, pressure is monitored periodically. In some embodiments, pressure is monitored continuously.

In some embodiments, pressure is selected via a control on a vacuum device. In some such embodiments, actual applied pressure is not separately monitored. In some such embodiments, actual applied pressure is separately monitored.

To begin the filtration the filter is filled slowly so that gas is not entrained in the solution, (e.g., pre-coat) and all of the air forced from the filter vessel. In some embodiments, the filter is pre-filled with the peptide mixture by automatic and/or manual addition of the mixture to filter housing. Automatic addition of peptide mixture to filter housing can be done 0.05 MPa or less. In some embodiments, a pump, separate from a primary filtration pump is used to fill the filtration vessel. Additional methods can be used to generate pressure, including but not limited to gravity, compressed gas (e.g., air).

The filter, membrane or otherwise may run in a dead-end or normal flow (NF) format or a tangential flow (TFF) format. Typically, normal flow may be preferred to ensure proper sterilization and maximize efficacy of the filtration step. The choice is dependent on a number of factors, primarily the users preference or installed filtration. A TFF process and equipment may be preferred when large amounts of peptide are to be recovered as TFF is less subject to clogging or fouling than NF methods.

Temperatures during filtration can also be optionally controlled. Viscosity of the peptide solutions varies based on temperature and viscosity, in turn, affects filtration efficiency and efficacy. In some embodiments, the temperature during filtration ranges from about 0° C. and about 40° C. (e.g., about 10, 20, 30° C.). The temperature during filtration can also be optionally controlled to prevent degradation of the peptides (e.g., the temperature should not exceed 100° C.

Filter and related equipment can all be autoclavable and/or steamed. To maintain a sterile filtered solution, the solution is captured from the fiber into a sterile bag (e.g., the Millipore Mobius) or a sterile stainless tank which is connected to the outlet of the filter. Further disposable equipment (i.e., figure media, housings, etc.) may be employed to ensure sterility.

In some embodiments, to ensure substantially all of the peptide mixture is fed to the filter, a scraper is used within the filtration feed tank to remove any peptide mixture that adheres to the surface of the tank. If a scraper is not used for self-assembling peptide mixture, the mixture is left in mortar-shape in the tank because compressed peptide mixture become like a gel. Alternatively a pipeline aide may be used (e.g., a pipe pig). The peptide mixture is filter through filter at a pressure of between about 0.1 and about 1 MPa (e.g., about 0.5 MPa). The flow rate of the filtration is between about 0.5 and about 5 liters per minute. Our work has revealed that the pressure during filtration can vary with the flow rate appears to have a larger influence on the efficacy of the filtration operation.

The filter can be operated in a counter pressure mode, which results in a pressure at the outlet of the filter greater than atmospheric. To apply counter pressure to filter effectively and avoid pressure being lowered, an additional tank between pressure source and filtration feed tank can be available since the pressure of compressed gas will be lower due to inflation in airspace of the filtration feed tank. Counter pressure can be applied by any suitable source, for example, a conventional valve, flow constriction (e.g., an orifice plate), pressure regulator. A positive pressure (e.g., inlet pressure>outlet pressure) drives the peptide solution through the filter. The pressure differential, in some embodiments, may be low with suitable maximum pressure differential depending on a variety of factor include the concentration and type of peptides to be filtered. In some embodiments, the pressure differential is between about 0.01 MPa and about 1 MPa (e.g., about 0.5 MPa).

At such differential pressure, the flow rate across the filter is low enough to generate a low-shear environment that does not substantially damage the peptides in solutions. Furthermore, the low shear environment does not limit the filtration process (e.g., limit filtration efficiency or efficacy by viscosity effects, clogging or generate air pockets in the filter).

After filtration, the filter might be damaged by high pressure; in many embodiments, it will be appropriate or desirable to examine the filter by integrity test in order to assess whether damaged might have compromised quality of the sterilization. In many embodiments, the filter will be washed (e.g., by water and in particular e.g., by hot water and/or by high-pressure water) prior to an integrity test. In some embodiments, such washing removes or may remove solution that may have remained in the filter, it being appreciated that such remaining solution can sometimes affect test data. In some embodiments, a filter is washed with steam and/or by autoclaving. In some embodiments, the process utilized to wash the filter may degrade peptide remaining in the filter. For example, in some embodiments, a method (e.g., including washing with water [e.g., high pressure and/or hot water], washing with steam, autoclaving, etc.) is performed under conditions and for a time sufficient to degrade such peptide. In some embodiments, a filter is washed with water having a temperature within the range of about 70° C. to 80° C., inclusive, prior to an integrity test. In some certain embodiments, a filter is washed with water having a temperature of about 70° C. prior to an integrity test.

Second Deaeration

After filtration the peptide solution undergoes a degassing step. In this second degassing step, the now sterile mixture should be protected from any contamination, such as metallic fine particle from driving parts. Thus, the second degassing may be performed without further equipment (e.g., rotary impeller) coming in contact with the peptide solution. In some embodiments, the solution is degassed by degassing methods described above (e.g., depressurization/vacuum, vibration, settling).

In some embodiments, the mixture is degassed by vibration to lower the viscosity of peptide mixture. In some embodiments, vibration can be induced by an orbital shaker. In some embodiments, the degassing vibration movement is in more than one dimension. For example, the vessel containing sterilized peptide solution is move in the x-axis and the y-axis (and/or optionally a z-axis). This is in comparison to simple, one dimension (or single axis) vibration (i.e., shaking). In some embodiments, pressure reduction can be combined with vibration for effective deaeration.

The device vibrational motion is provided with a means for varying both the rotational speed and distance that the device moves in any particular direction. In some embodiments, the vibration frequency is about 50 cycles per minute and any particular direction. In some embodiments, the vibration frequency ranges from between about 20 cycles per minute to about 360 revolutions per minute, e.g., about 30, 40, 50, 60, 90, 100, 120, 150, 180, 210, 240, 300, 360). The circular direction of vibration is clockwise or counterclockwise or combination of both. In some embodiments, the distance of the vibration motion is between about-20 cm and about 20 cm.

In some embodiments, the deaerating step is performed by vacuum. The pressure of the solution is reduced by at least about −0.05 MPa (e.g., −0.01 MPa, −0.015 MPa, −0.02 MPa, −0.025 MPa). We have realized that the rate of reduction of pressure (or increase in vacuum) effects the efficacy and efficiency of the deaerating process. In some embodiments, the rate of pressure reduction is not more than about −0.01 MPa/minute (e.g., about −0.005 MPa/minute, about −0.0025 MPa/minute, about −0.001 MPa/minute, and ranges there between). In some embodiments, the rate of pressure reduction is dependent upon the total volume of the solution to be deaerated.

The second Deaeration step also results in a uniformly mixed solution.

Exemplary vibration degassing equipment includes device models from Medical & Food System Co., Ltd. (JPO patent application #2010-161052; publication #2012-11364).

Filling

After the second degassing step, the peptide mixture is suitable for filling into a syringe. The syringe can be any size, e.g., 1 mL, 2 mL, 3 mL, 5 mL, 10 mL. Further, syringes can be any material of construction (e.g., glass, polyethylene, etc.). Proper filling is determined based on visual inspection, weighing. The target volume for each syringe depends on the viscosity of the solution.

Syringes are placed in a filing station and sterilized peptide solution is pumped into the syringe in the desired volumes. In some embodiments, a vacuum is then applied to the syringe after the peptide solution is introduced, but before the plunger is added. The rate of vacuum is partially dependent on the viscosity and boiling point of the peptide solution. The rate of application of vacuum can be selected so that its application does not introduce air bubbles into the peptide solution. A further aspect of filling syringes includes placing the plunger in the syringe. The plunger should be placed so that it is in contact with the peptide mixture, but without trapping air between the peptide mixture and the plunger and without the disturbing the peptide mixture to such an extent that the solution splatters within a syringe or air is incorporated in the peptide mixture.

After the syringe is filled, it is visually inspected for (a) any foreign substances or visible contaminants (b) any flaws, damage or defects to the syringe itself; and (c) any leaks. In process, inspection includes but is not limited to peptide concentration measured with UV-spectroscopic method and/or overall nitrogen content, HPLC, mass spectrogram, pH, gelation and/or viscosity, bacterial contamination and endotoxin, heavy-metal determination, residual solvent measurement. These inspection parameters can be performed repeatedly throughout the process and after the fill-finish process is complete as a final quality control. The syringe then undergoes a final assembly which may include addition of the plunger, grip and affixing a label. Syringes may be packaged into multi-unit packages (e.g., 1, 2, 3, 4, 5, etc., unit pillow or blister packs) for shipping and storage. Double packaging is also available to avoid bacterial contamination of syringe surface before use in operation room.

After packaging, the packs are sterilized by ethylene oxide gas (“EOG”) or hydrogen peroxide gas sterilization. After each step, or after a batch of peptide solution has been processed, the process equipment can be cleaned, according to cGMP standards. The equipment can be cleaned in place, or disassembled and cleaned piece-by-piece. Additionally, process equipment can be sterilized by common sterilization techniques (e.g., autoclaving, irradiation, EOG, etc.).

Cleaning Equipments

Highly viscous peptide mixture is often sticking to surface of tank and pipeline. Cleaning all the equipments following cGMP is so hard for the sticky peptide mixture that manufacturers look for effective cleaning method. Since peptide is generally degraded by exposure to high temperature (e.g., 121° C.), steam or hot water is available for removing peptide mixture from the surface of tank and pipeline. Exposure to steam in clean-in-place (CIP) and autoclave of separated equipments are effective to clean the equipments. Since self-assemble peptide is also degradable by steam or autoclave, the peptide after exposure to steam or autoclave can be removable by rinsing with water. Remaining peptide on equipment can be checked by total organic carbon (TOC) measurement and cleaning efficiency can be validated by TOC, following cGMP.

Example Exemplary Production Validation of a Self-Assembling Peptide Solution

This Example illustrates production of a self-assembling peptide solution employing methods comprising a first deaerating step wherein a peptide solution is deaerated by lowering the pressure, filtering the mixture through a sterilizing filter, and a second deaerating step wherein the filtrate is deaerated by vibration and lowering the pressure.

Briefly, a 2.5% peptide solution was produced on a 10 L batch scale using raw peptide Ac-(RADA)₄-NH₂ (unmodified sequence shown in SEQ ID NO:1) (lot #12103001). Exemplary production conditions were as follows:

Dissolution (60 minutes): 10 kg water for injection, 256.7 grams of peptide and an impeller revolution rate of 300 to 500 rpm.

A first deaeration step (60 minutes): an air vacuum of −0.099 MPa to −0.100 MPa and an impeller revolution rate of 250 rpm.

A filtration step: a 20″ cartridge, 0.2 μm mesh sterile filter (Millipore Express SHF), a pre-filling pressure of 0.05 MPa, a counter filtration pressure of 0.5 MPa, a scraper diameter of 35 cm (similar to that of a dissolving tank), a pressure source tank having a capacity of 40 L, and a washing filter for an integrity test (Pure steam at 100° C.-130° C. for 30 minutes) using an integrity test instrument (INTEGRITEST®4 System, Millipore). Peptide solution on the filter is washed prior to an integrity test (e.g., by water and in particular e.g., by hot water and/or by high-pressure water).

A second deaeration step (60 minutes): an air vacuum of 0.099 MPa to −0.100 MPa, a circular revolution rate of 100 rpm and a vibration mode distance of 10 cm.

The resulting peptide solution was employed to fill articles using a high speed filling machine. For example, syringes were filled using a 10I/10FF/10I machine (KT Manufacturing Co. Ltd.) at a rate of 1000 articles/hour utilizing two filling nozzles. The production of 1 mL (574 articles), 3 mL (1164 articles), and 5 mL (250 articles) variations were subjected to ethylene oxide gas for final sterilization.

Taken together, this example demonstrates that methods to manufacture and purify peptide solutions as described herein effectively provide peptide solutions suitably packaged for a variety of scientific and medical applications without any degradation or physical changes to the peptide mixtures.

Having thus described several aspects of at least one embodiment of this invention, it is to be appreciated that various alterations, modifications, and improvements will readily occur to those skilled in the art. Such alterations, modifications, and improvements are intended to be part of this disclosure, and are intended to be within the spirit and scope of the invention. Accordingly, the foregoing description and drawings are by way of example only and the invention is described in detail by the claims that follow.

Use of ordinal terms such as “first,” “second,” “third,” etc., in the claims to modify a claim element does not by itself connote any priority, precedence, or order of one claim element over another or the temporal order in which acts of a method are performed, but are used merely as labels to distinguish one claim element having a certain name from another element having a same name (but for use of the ordinal term) to distinguish the claim elements.

The articles “a” and “an” as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to include the plural referents. Claims or descriptions that include “or” between one or more members of a group are considered satisfied if one, more than one, or all of the group members are present in, employed in, or otherwise relevant to a given product or process unless indicated to the contrary or otherwise evident from the context. The invention includes embodiments in which exactly one member of the group is present in, employed in, or otherwise relevant to a given product or process. The invention also includes embodiments in which more than one, or the entire group members are present in, employed in, or otherwise relevant to a given product or process. Furthermore, it is to be understood that the invention encompasses all variations, combinations, and permutations in which one or more limitations, elements, clauses, descriptive terms, etc., from one or more of the listed claims is introduced into another claim dependent on the same base claim (or, as relevant, any other claim) unless otherwise indicated or unless it would be evident to one of ordinary skill in the art that a contradiction or inconsistency would arise. Where elements are presented as lists, (e.g., in Markush group or similar format) it is to be understood that each subgroup of the elements is also disclosed, and any element(s) can be removed from the group. It should be understood that, in general, where the invention, or aspects of the invention, is/are referred to as comprising particular elements, features, etc., certain embodiments of the invention or aspects of the invention consist, or consist essentially of, such elements, features, etc. For purposes of simplicity those embodiments have not in every case been specifically set forth in so many words herein. It should also be understood that any embodiment or aspect of the invention can be explicitly excluded from the claims, regardless of whether the specific exclusion is recited in the specification. The publications, websites and other reference materials referenced herein to describe the background of the invention and to provide additional detail regarding its practice are hereby incorporated by reference. 

1. A method for deaerating and sterilizing a self-assembling peptide solution having at least 0.5% weight percent of a self-assembling peptide, the method comprising the steps of: a first deaerating step wherein the self-assembling peptide solution is deaerated by lowering a pressure on the self-assembling peptide solution to vacuum; filtering the self-assembling peptide solution through a sterilizing filter thereby producing a self-assembling peptide filtrate; and a second deaerating step wherein the filtrate is deaerated by vibration at a vibration frequency between 20 and 360 revolutions per minute, and by lowering the pressure on the self-assembling peptide solution filtrate by at least 0.05 MPa.
 2. The method of claim 1, wherein the sterilizing filter has an average pore size of less than 0.22 μm.
 3. The method of claim 1, wherein the self-assembling peptide comprises one of RADA16-I (SEQ ID NO:1), IEIK13 (SEQ ID NO:39); and KLDL12 (SEQ ID NO:12).
 4. The method of claim 1, wherein the first deaerating step comprises lowering the pressure at a rate of less than 0.01 MPa/min.
 5. The method of claim 1, wherein the first deaerating step occurs in a deaeration chamber and comprises lowering the pressure by at least 0.095 MPa.
 6. The method of claim 5, wherein the pressure is lowered by at least 0.095 MPa for at least 30 minutes.
 7. The method of claim 1, wherein an eccentric distance of the vibration is between −10 cm and 10 cm.
 8. The method of claim 1, wherein the second deaerating step comprises lowering the pressure by at least 0.095 MPa.
 9. The method of claim 1, wherein a step of sterilizing is performed with one of ethylene oxide gas and a hydrogen peroxide gas.
 10. The method of claim 1, wherein the sterilizing filter is constructed from a material selected from the group consisting of the following: cellulose nitrate, cellulose acetate, vinyl polymers, fluorocarbons, polyethylene, ultrahigh molecular weight polyethylene, polypropylene, EVA copolymers and alpha olefins, metallocene olefinic polymers, PFA, MFA, PTFE, polycarbonates, vinyl copolymers, polyamides, nylon, polyesters, cellulose, regenerated cellulose, cellulose composites, polysulfone, polyethersulfone, polyarylsulfone, polyphenylsulfone, polyacrylonitrile, polyvinylidene fluoride (PVDF), and blends thereof.
 11. The method of claim 1, wherein the sterilizing filter is constructed from polyethersulfone.
 12. The method of claim 1, wherein the filtering step comprises a step of filling the sterilizing filter at a first pressure, then increasing the pressure to perform the filtration.
 13. The method of claim 1, wherein the sterilizing filter is washed prior to an integrity test.
 14. The method of claim 14, wherein the sterilizing filter is washed with water prior to an integrity test, and the water is one of above 70° C. and high-pressure, or both.
 15. The method of claim 1, wherein the filtration step is performed with two filters operating in parallel. 